Last synced on 20 December 2024 at 11:05 pm

Vaginal Hydrogel Packing System

Page Type
Product Code
Definition
A vaginal hydrogel packing system is a non-powered positioning device composed of a flexible container filled with a hydrogel. The device is intended to reduce the radiation dose delivered to adjacent pelvic organs by temporarily displacing the vaginal wall and adjacent pelvic tissues during radiation therapy treatment planning and delivery.
Physical State
Flexible container filled with hydrogel to create space in the vaginal cavity
Technical Method
Placed in the vaginal cavity for radiation therapy treatment. The hydrogel material is injected into a flexible container, which creates space within the vaginal cavity to aid in the reduction of dose to adjacent pelvic organs during radiation therapy.
Target Area
Vaginal cavity
Regulation Medical Specialty
Radiology
Review Panel
Radiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
892.5735
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QXR is linked to regulation 21CFR892.5735, which does not seem to exist yet. It may be pending at the moment.

Vaginal Hydrogel Packing System

Page Type
Product Code
Definition
A vaginal hydrogel packing system is a non-powered positioning device composed of a flexible container filled with a hydrogel. The device is intended to reduce the radiation dose delivered to adjacent pelvic organs by temporarily displacing the vaginal wall and adjacent pelvic tissues during radiation therapy treatment planning and delivery.
Physical State
Flexible container filled with hydrogel to create space in the vaginal cavity
Technical Method
Placed in the vaginal cavity for radiation therapy treatment. The hydrogel material is injected into a flexible container, which creates space within the vaginal cavity to aid in the reduction of dose to adjacent pelvic organs during radiation therapy.
Target Area
Vaginal cavity
Regulation Medical Specialty
Radiology
Review Panel
Radiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
892.5735
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QXR is linked to regulation 21CFR892.5735, which does not seem to exist yet. It may be pending at the moment.